A medical records based study for prediction of high-risk human papillomavirus infection natural outcome based on viral load

A study for prediction of high-risk human papillomavirus infection natural outcome based on the synchronous HPV genotyping and quantification assay

Status

Recruiting

Phases

Early Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR2000028948

Enrollment

Unknown

Registered

2020-01-08

Start date

2020-02-07

Completion date

Unknown

Last updated

2020-02-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

high-risk human papillomavirus infection

Interventions

Case series:none

Eligibility

Sex/Gender

Female

Age

21 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Aged 21-65 year old women living in Chongqing with sexual life; 2. women with single type HPV infection for the first time; 3. Subjects with follow-up conditions that volunteering to participate in it and have signed informed consent.

Exclusion criteria

Exclusion criteria: 1. history of cervical precancerous lesions and cervical cancer; 2. immunosuppressive patients; 3. smokers; 4, history of malignant tumors; 5. pregnancy or has pregnancy plan; 6. HPV infection drug intervention.

Design outcomes

Primary

Measure	Time frame
HPV viral load;	—

Countries

China

Contacts

Public ContactLong Xin

Chongqing Health Center for Woman and Children

4261749@qq.com+86 13608385160

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026